Macrocyclic derivatives of isosteviol with two tetracyclic diterpenoid skeletons
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[1] V. M. Babaev,et al. Synthesis and antituberculosis activity of novel unfolded and macrocyclic derivatives of ent-kaurane steviol. , 2012, Bioorganic & medicinal chemistry letters.
[2] K. Petrov,et al. Unfolded and macrocyclic ammonium derivatives of diterpenoids steviol and isosteviol having choline moieties. Synthesis and inhibitory activities toward acetylcholine- and butyrylcholinesterases , 2012 .
[3] A. Gubaidullin,et al. Synthesis of macrocycles with one and more ent-beyerane skeletons based on the diterpenoid isosteviol , 2011, Chemistry of Natural Compounds.
[4] V. Gubskaya,et al. New malonate macrocycle bearing two isosteviol moieties and its adduct with fullerene C60 , 2011 .
[5] Jun-qing Chen,et al. The Synthesis and Crystal Structure of (4α,8β,13β,16β)-13-Methyl-16,18-diol-17-Norkaurane: A Simultaneous Reduction Product of Isosteviol , 2011 .
[6] G. Dai,et al. Stereoselective Synthesis, Characterization, and Antibacterial Activities of Novel Isosteviol Derivatives with D-Ring Modification , 2010 .
[7] Chao Pi,et al. Simple amphiphilic isosteviol–proline conjugates as chiral catalysts for the direct asymmetric aldol reaction in the presence of water , 2010 .
[8] A. Gubaidullin,et al. New synthesis of diterpenoid (16S)-dihydrosteviol , 2009 .
[9] I. Ojima,et al. Recent advances in the chemistry and biology of new generation taxoids. , 2009, Journal of natural products.
[10] G. Dai,et al. Stereoselective synthesis of 15- and 16-substituted isosteviol derivatives and their cytotoxic activities. , 2009, Bioorganic & medicinal chemistry letters.
[11] G. Dai,et al. Stereoselective synthesis of bioactive isosteviol derivatives as alpha-glucosidase inhibitors. , 2009, Bioorganic & medicinal chemistry.
[12] V. Chatsudthipong,et al. A Natural Plant-Derived Dihydroisosteviol Prevents Cholera Toxin-Induced Intestinal Fluid Secretion , 2008, Journal of Pharmacology and Experimental Therapeutics.
[13] A. Gubaidullin,et al. First synthetic macrocyclic compounds in the series of ent-beyerane diterpenoids , 2007 .
[14] O. Andreeva,et al. Alkylation of the isosteviol terpenoid and its oxime with dibromoalkanes in the KOH-DMSO system , 2007 .
[15] S. V. Larionov,et al. A chiral pentadentate macrocyclic ligand (L) based on the natural monoterpene (-)-α-pinene and the seven-coordinate cobalt compound [CoL(NO3)]NO3 , 2006 .
[16] O. Fedorova,et al. Synthesis and anti-tuberculous activity of diesters based on isosteviol and dicarboxylic acids , 2006, Pharmaceutical Chemistry Journal.
[17] J. Geuns,et al. Steviol quantification at the picomole level by high-performance liquid chromatography. , 2004, Journal of agricultural and food chemistry.
[18] A. Gubaidullin,et al. Chemistry and Structure of Diterpene Compounds of the Kaurane Series: VI. Isosteviol Esters , 2003 .
[19] I. Ojima,et al. Macrocycle Formation by Ring-Closing Metathesis. Application to the Syntheses of Novel Macrocyclic Taxoids , 2000 .